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You searched for subject:(borylation). Showing records 1 – 30 of 53 total matches.

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University of California – San Diego

1. Romero, Erik Anthony. Taming Carbene Copper(I)-Hydride Complexes.

Degree: Chemistry and Biochemistry, 2019, University of California – San Diego

 Although initially reported in 1844, copper(I)-hydrides were not widely studied until the isolation of “Stryker’s reagent” in 1971. Following this development, researchers reported a myriad… (more)

Subjects/Keywords: Inorganic chemistry; borylation; carbene; copper; hydride; monomer

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APA (6th Edition):

Romero, E. A. (2019). Taming Carbene Copper(I)-Hydride Complexes. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/0574f1cg

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Romero, Erik Anthony. “Taming Carbene Copper(I)-Hydride Complexes.” 2019. Thesis, University of California – San Diego. Accessed October 21, 2019. http://www.escholarship.org/uc/item/0574f1cg.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Romero, Erik Anthony. “Taming Carbene Copper(I)-Hydride Complexes.” 2019. Web. 21 Oct 2019.

Vancouver:

Romero EA. Taming Carbene Copper(I)-Hydride Complexes. [Internet] [Thesis]. University of California – San Diego; 2019. [cited 2019 Oct 21]. Available from: http://www.escholarship.org/uc/item/0574f1cg.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Romero EA. Taming Carbene Copper(I)-Hydride Complexes. [Thesis]. University of California – San Diego; 2019. Available from: http://www.escholarship.org/uc/item/0574f1cg

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Virginia Tech

2. Snead, Russell Franklin. Development of Novel, Regioselective Borylation Protocols.

Degree: PhD, Chemistry, 2018, Virginia Tech

 Organoboron compounds are highly valued synthetic intermediates due to their diverse array of reactivity, which is often utilized in the synthesis of valuable organic molecules.… (more)

Subjects/Keywords: borylation; transition metal-catalyzed; transition metal-free; allenes; alkynamides

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APA (6th Edition):

Snead, R. F. (2018). Development of Novel, Regioselective Borylation Protocols. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/85003

Chicago Manual of Style (16th Edition):

Snead, Russell Franklin. “Development of Novel, Regioselective Borylation Protocols.” 2018. Doctoral Dissertation, Virginia Tech. Accessed October 21, 2019. http://hdl.handle.net/10919/85003.

MLA Handbook (7th Edition):

Snead, Russell Franklin. “Development of Novel, Regioselective Borylation Protocols.” 2018. Web. 21 Oct 2019.

Vancouver:

Snead RF. Development of Novel, Regioselective Borylation Protocols. [Internet] [Doctoral dissertation]. Virginia Tech; 2018. [cited 2019 Oct 21]. Available from: http://hdl.handle.net/10919/85003.

Council of Science Editors:

Snead RF. Development of Novel, Regioselective Borylation Protocols. [Doctoral Dissertation]. Virginia Tech; 2018. Available from: http://hdl.handle.net/10919/85003

3. Charbonnier, Jean-Baptiste. Réaction de nitration en continu pour la synthèse d’un principe actif pharmaceutique : fonctionnalisation d’hétérocycles borés obtenus par borylation électrophile : Continuous nitration reaction for the synthesis of an active pharmaceutical ingredient : functionnalisation of boron heterocycles synthetised by electrophilic borylation.

Degree: Docteur es, Chimie organique, 2018, Bordeaux

La fluidique est un outil offrant des avantages industriels notamment en termes de sécurité grâce à un meilleur contrôle thermique mais aussi une diminution des… (more)

Subjects/Keywords: Microfluidique; Principe actif pharmaceutique; Nitration d'alcool; Micromélangeur; Borylation électrophile; Oxaborinine; Complexe amine-borane; Microfluidic; Active pharmaceutical ingredient; Alcohol nitration; Micromixer; Electrophilic borylation; Oxaborinin; Amine-borane complex

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APA (6th Edition):

Charbonnier, J. (2018). Réaction de nitration en continu pour la synthèse d’un principe actif pharmaceutique : fonctionnalisation d’hétérocycles borés obtenus par borylation électrophile : Continuous nitration reaction for the synthesis of an active pharmaceutical ingredient : functionnalisation of boron heterocycles synthetised by electrophilic borylation. (Doctoral Dissertation). Bordeaux. Retrieved from http://www.theses.fr/2018BORD0078

Chicago Manual of Style (16th Edition):

Charbonnier, Jean-Baptiste. “Réaction de nitration en continu pour la synthèse d’un principe actif pharmaceutique : fonctionnalisation d’hétérocycles borés obtenus par borylation électrophile : Continuous nitration reaction for the synthesis of an active pharmaceutical ingredient : functionnalisation of boron heterocycles synthetised by electrophilic borylation.” 2018. Doctoral Dissertation, Bordeaux. Accessed October 21, 2019. http://www.theses.fr/2018BORD0078.

MLA Handbook (7th Edition):

Charbonnier, Jean-Baptiste. “Réaction de nitration en continu pour la synthèse d’un principe actif pharmaceutique : fonctionnalisation d’hétérocycles borés obtenus par borylation électrophile : Continuous nitration reaction for the synthesis of an active pharmaceutical ingredient : functionnalisation of boron heterocycles synthetised by electrophilic borylation.” 2018. Web. 21 Oct 2019.

Vancouver:

Charbonnier J. Réaction de nitration en continu pour la synthèse d’un principe actif pharmaceutique : fonctionnalisation d’hétérocycles borés obtenus par borylation électrophile : Continuous nitration reaction for the synthesis of an active pharmaceutical ingredient : functionnalisation of boron heterocycles synthetised by electrophilic borylation. [Internet] [Doctoral dissertation]. Bordeaux; 2018. [cited 2019 Oct 21]. Available from: http://www.theses.fr/2018BORD0078.

Council of Science Editors:

Charbonnier J. Réaction de nitration en continu pour la synthèse d’un principe actif pharmaceutique : fonctionnalisation d’hétérocycles borés obtenus par borylation électrophile : Continuous nitration reaction for the synthesis of an active pharmaceutical ingredient : functionnalisation of boron heterocycles synthetised by electrophilic borylation. [Doctoral Dissertation]. Bordeaux; 2018. Available from: http://www.theses.fr/2018BORD0078

4. Peck, Cheryl Lynne. Development of Transition Metal-Catalyzed Borylation Protocols using Symmetrical and Unsymmetrical Diboron Reagents.

Degree: PhD, Chemistry, 2017, Virginia Tech

 The versatility of organoboron compounds has been demonstrated by their use as synthetic intermediates and more recently in therapeutic applications since the FDA approval of… (more)

Subjects/Keywords: borylation; transition metal-catalyzed; conjugate addition; alkynes; diboron reagents

…15 Chapter 2. Copper(II)-catalyzed β-borylation of acetylenic esters in water… …34 2.4 Optimizing the β-borylation of alkynoates with B2pin2… …37 2.6 Substrate scope for the copper(II)-catalyzed β-borylation of alkynoates… …52 3.4 Optimizing the β-borylation of ethyl 2-butynoate with pinB-Bdan… …55 3.5 Substrate scope for the β-borylation of alkynoates with pinB-Bdan… 

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APA (6th Edition):

Peck, C. L. (2017). Development of Transition Metal-Catalyzed Borylation Protocols using Symmetrical and Unsymmetrical Diboron Reagents. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/80343

Chicago Manual of Style (16th Edition):

Peck, Cheryl Lynne. “Development of Transition Metal-Catalyzed Borylation Protocols using Symmetrical and Unsymmetrical Diboron Reagents.” 2017. Doctoral Dissertation, Virginia Tech. Accessed October 21, 2019. http://hdl.handle.net/10919/80343.

MLA Handbook (7th Edition):

Peck, Cheryl Lynne. “Development of Transition Metal-Catalyzed Borylation Protocols using Symmetrical and Unsymmetrical Diboron Reagents.” 2017. Web. 21 Oct 2019.

Vancouver:

Peck CL. Development of Transition Metal-Catalyzed Borylation Protocols using Symmetrical and Unsymmetrical Diboron Reagents. [Internet] [Doctoral dissertation]. Virginia Tech; 2017. [cited 2019 Oct 21]. Available from: http://hdl.handle.net/10919/80343.

Council of Science Editors:

Peck CL. Development of Transition Metal-Catalyzed Borylation Protocols using Symmetrical and Unsymmetrical Diboron Reagents. [Doctoral Dissertation]. Virginia Tech; 2017. Available from: http://hdl.handle.net/10919/80343


Kyoto University

5. Ishibashi, Aoi. Synthesis and Transformation of Organoboronic Acids Using Boron-Modifying Strategy for Catalytic C-H Functionalization .

Degree: 2017, Kyoto University

Subjects/Keywords: Organoboronic Acid; C?H Functionalization; C?H Borylation; Hydroarylation; Oligo(naphthalene-2, 3-diyl)s

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APA (6th Edition):

Ishibashi, A. (2017). Synthesis and Transformation of Organoboronic Acids Using Boron-Modifying Strategy for Catalytic C-H Functionalization . (Thesis). Kyoto University. Retrieved from http://hdl.handle.net/2433/225960

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Ishibashi, Aoi. “Synthesis and Transformation of Organoboronic Acids Using Boron-Modifying Strategy for Catalytic C-H Functionalization .” 2017. Thesis, Kyoto University. Accessed October 21, 2019. http://hdl.handle.net/2433/225960.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Ishibashi, Aoi. “Synthesis and Transformation of Organoboronic Acids Using Boron-Modifying Strategy for Catalytic C-H Functionalization .” 2017. Web. 21 Oct 2019.

Vancouver:

Ishibashi A. Synthesis and Transformation of Organoboronic Acids Using Boron-Modifying Strategy for Catalytic C-H Functionalization . [Internet] [Thesis]. Kyoto University; 2017. [cited 2019 Oct 21]. Available from: http://hdl.handle.net/2433/225960.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Ishibashi A. Synthesis and Transformation of Organoboronic Acids Using Boron-Modifying Strategy for Catalytic C-H Functionalization . [Thesis]. Kyoto University; 2017. Available from: http://hdl.handle.net/2433/225960

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Kyoto University / 京都大学

6. Ishibashi, Aoi. Synthesis and Transformation of Organoboronic Acids Using Boron-Modifying Strategy for Catalytic C-H Functionalization : ホウ素修飾法に基づいた触媒的C-H官能基化による有機ホウ素化合物の合成と変換.

Degree: 博士(工学), 2017, Kyoto University / 京都大学

新制・課程博士

甲第20584号

工博第4364号

Subjects/Keywords: Organoboronic Acid; C?H Functionalization; C?H Borylation; Hydroarylation; Oligo(naphthalene-2, 3-diyl)s

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APA (6th Edition):

Ishibashi, A. (2017). Synthesis and Transformation of Organoboronic Acids Using Boron-Modifying Strategy for Catalytic C-H Functionalization : ホウ素修飾法に基づいた触媒的C-H官能基化による有機ホウ素化合物の合成と変換. (Thesis). Kyoto University / 京都大学. Retrieved from http://hdl.handle.net/2433/225960 ; http://dx.doi.org/10.14989/doctor.k20584

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Ishibashi, Aoi. “Synthesis and Transformation of Organoboronic Acids Using Boron-Modifying Strategy for Catalytic C-H Functionalization : ホウ素修飾法に基づいた触媒的C-H官能基化による有機ホウ素化合物の合成と変換.” 2017. Thesis, Kyoto University / 京都大学. Accessed October 21, 2019. http://hdl.handle.net/2433/225960 ; http://dx.doi.org/10.14989/doctor.k20584.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Ishibashi, Aoi. “Synthesis and Transformation of Organoboronic Acids Using Boron-Modifying Strategy for Catalytic C-H Functionalization : ホウ素修飾法に基づいた触媒的C-H官能基化による有機ホウ素化合物の合成と変換.” 2017. Web. 21 Oct 2019.

Vancouver:

Ishibashi A. Synthesis and Transformation of Organoboronic Acids Using Boron-Modifying Strategy for Catalytic C-H Functionalization : ホウ素修飾法に基づいた触媒的C-H官能基化による有機ホウ素化合物の合成と変換. [Internet] [Thesis]. Kyoto University / 京都大学; 2017. [cited 2019 Oct 21]. Available from: http://hdl.handle.net/2433/225960 ; http://dx.doi.org/10.14989/doctor.k20584.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Ishibashi A. Synthesis and Transformation of Organoboronic Acids Using Boron-Modifying Strategy for Catalytic C-H Functionalization : ホウ素修飾法に基づいた触媒的C-H官能基化による有機ホウ素化合物の合成と変換. [Thesis]. Kyoto University / 京都大学; 2017. Available from: http://hdl.handle.net/2433/225960 ; http://dx.doi.org/10.14989/doctor.k20584

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Illinois – Chicago

7. Mazzacano, Thomas J. New Developments in Base Metal-Catalyzed C-H Borylation.

Degree: 2017, University of Illinois – Chicago

 The catalytic functionalization of carbon-hydrogen bonds to form carbon-boron bonds is an emerging field in organometallic chemistry. Substrates containing carbon-boron bonds play a pivotal role… (more)

Subjects/Keywords: Base Metals Organometallic C-H Borylation Catalysis Catalyst

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APA (6th Edition):

Mazzacano, T. J. (2017). New Developments in Base Metal-Catalyzed C-H Borylation. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/22071

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Mazzacano, Thomas J. “New Developments in Base Metal-Catalyzed C-H Borylation.” 2017. Thesis, University of Illinois – Chicago. Accessed October 21, 2019. http://hdl.handle.net/10027/22071.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Mazzacano, Thomas J. “New Developments in Base Metal-Catalyzed C-H Borylation.” 2017. Web. 21 Oct 2019.

Vancouver:

Mazzacano TJ. New Developments in Base Metal-Catalyzed C-H Borylation. [Internet] [Thesis]. University of Illinois – Chicago; 2017. [cited 2019 Oct 21]. Available from: http://hdl.handle.net/10027/22071.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Mazzacano TJ. New Developments in Base Metal-Catalyzed C-H Borylation. [Thesis]. University of Illinois – Chicago; 2017. Available from: http://hdl.handle.net/10027/22071

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Kyoto University / 京都大学

8. Yamamoto, Yutaro. Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents : ルイス酸性を有するホウ素反応剤や有機ケイ素反応剤を用いたパラジウム触媒による塩化アリールの変換反応に関する研究.

Degree: 博士(理学), 2017, Kyoto University / 京都大学

新制・課程博士

甲第20205号

理博第4290号

Subjects/Keywords: palladium; aryl chloride; borylation; hydrodechlorination; cross-coupling reactions

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APA (6th Edition):

Yamamoto, Y. (2017). Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents : ルイス酸性を有するホウ素反応剤や有機ケイ素反応剤を用いたパラジウム触媒による塩化アリールの変換反応に関する研究. (Thesis). Kyoto University / 京都大学. Retrieved from http://hdl.handle.net/2433/225430 ; http://dx.doi.org/10.14989/doctor.k20205

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Yamamoto, Yutaro. “Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents : ルイス酸性を有するホウ素反応剤や有機ケイ素反応剤を用いたパラジウム触媒による塩化アリールの変換反応に関する研究.” 2017. Thesis, Kyoto University / 京都大学. Accessed October 21, 2019. http://hdl.handle.net/2433/225430 ; http://dx.doi.org/10.14989/doctor.k20205.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Yamamoto, Yutaro. “Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents : ルイス酸性を有するホウ素反応剤や有機ケイ素反応剤を用いたパラジウム触媒による塩化アリールの変換反応に関する研究.” 2017. Web. 21 Oct 2019.

Vancouver:

Yamamoto Y. Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents : ルイス酸性を有するホウ素反応剤や有機ケイ素反応剤を用いたパラジウム触媒による塩化アリールの変換反応に関する研究. [Internet] [Thesis]. Kyoto University / 京都大学; 2017. [cited 2019 Oct 21]. Available from: http://hdl.handle.net/2433/225430 ; http://dx.doi.org/10.14989/doctor.k20205.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Yamamoto Y. Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents : ルイス酸性を有するホウ素反応剤や有機ケイ素反応剤を用いたパラジウム触媒による塩化アリールの変換反応に関する研究. [Thesis]. Kyoto University / 京都大学; 2017. Available from: http://hdl.handle.net/2433/225430 ; http://dx.doi.org/10.14989/doctor.k20205

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Kyoto University

9. Yamamoto, Yutaro. Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents .

Degree: 2017, Kyoto University

Subjects/Keywords: palladium; aryl chloride; borylation; hydrodechlorination; cross-coupling reactions

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Yamamoto, Y. (2017). Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents . (Thesis). Kyoto University. Retrieved from http://hdl.handle.net/2433/225430

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Yamamoto, Yutaro. “Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents .” 2017. Thesis, Kyoto University. Accessed October 21, 2019. http://hdl.handle.net/2433/225430.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Yamamoto, Yutaro. “Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents .” 2017. Web. 21 Oct 2019.

Vancouver:

Yamamoto Y. Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents . [Internet] [Thesis]. Kyoto University; 2017. [cited 2019 Oct 21]. Available from: http://hdl.handle.net/2433/225430.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Yamamoto Y. Studies on Palladium-Catalyzed Reactions of Aryl Chlorides with Lewis Acidic Boron or Organosilicon Reagents . [Thesis]. Kyoto University; 2017. Available from: http://hdl.handle.net/2433/225430

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Universitat Rovira i Virgili

10. Zárate Sáez, Cayetana. C-heteroatom bond-formation via ni-catalyzed c-o bond cleavage.

Degree: Departament de Química Analítica i Química Orgànica, 2017, Universitat Rovira i Virgili

 While the field of cross-coupling has reached remarkable levels of sophistication, the vast majority of processes are still being conducted with organic halide counterparts. Drawbacks… (more)

Subjects/Keywords: Derivats del fenol; Catàlisi de Ni; Sililaciò y Borilaciò; Derivados del fenol; Sililación y borilación; Phenol derivatives; Ni catalysis; Silylation and borylation; Ciències; 547

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APA (6th Edition):

Zárate Sáez, C. (2017). C-heteroatom bond-formation via ni-catalyzed c-o bond cleavage. (Thesis). Universitat Rovira i Virgili. Retrieved from http://hdl.handle.net/10803/401555

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Zárate Sáez, Cayetana. “C-heteroatom bond-formation via ni-catalyzed c-o bond cleavage.” 2017. Thesis, Universitat Rovira i Virgili. Accessed October 21, 2019. http://hdl.handle.net/10803/401555.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Zárate Sáez, Cayetana. “C-heteroatom bond-formation via ni-catalyzed c-o bond cleavage.” 2017. Web. 21 Oct 2019.

Vancouver:

Zárate Sáez C. C-heteroatom bond-formation via ni-catalyzed c-o bond cleavage. [Internet] [Thesis]. Universitat Rovira i Virgili; 2017. [cited 2019 Oct 21]. Available from: http://hdl.handle.net/10803/401555.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Zárate Sáez C. C-heteroatom bond-formation via ni-catalyzed c-o bond cleavage. [Thesis]. Universitat Rovira i Virgili; 2017. Available from: http://hdl.handle.net/10803/401555

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Michigan

11. Schimler, Sydonie. Development of Practical Fluorination Methods and Selective C-H Borylation of Methane.

Degree: PhD, Chemistry, 2017, University of Michigan

 Fluorinated (hetero)arenes are finding increasing importance in pharmaceuticals and agrochemicals. As a result, the development of mild, inexpensive, and practical methods for the formation of… (more)

Subjects/Keywords: Fluorination; Borylation; Chemistry; Science

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APA (6th Edition):

Schimler, S. (2017). Development of Practical Fluorination Methods and Selective C-H Borylation of Methane. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/138679

Chicago Manual of Style (16th Edition):

Schimler, Sydonie. “Development of Practical Fluorination Methods and Selective C-H Borylation of Methane.” 2017. Doctoral Dissertation, University of Michigan. Accessed October 21, 2019. http://hdl.handle.net/2027.42/138679.

MLA Handbook (7th Edition):

Schimler, Sydonie. “Development of Practical Fluorination Methods and Selective C-H Borylation of Methane.” 2017. Web. 21 Oct 2019.

Vancouver:

Schimler S. Development of Practical Fluorination Methods and Selective C-H Borylation of Methane. [Internet] [Doctoral dissertation]. University of Michigan; 2017. [cited 2019 Oct 21]. Available from: http://hdl.handle.net/2027.42/138679.

Council of Science Editors:

Schimler S. Development of Practical Fluorination Methods and Selective C-H Borylation of Methane. [Doctoral Dissertation]. University of Michigan; 2017. Available from: http://hdl.handle.net/2027.42/138679


Princeton University

12. Obligacion, Jennifer Victoriano. BASE METAL CATALYSIS FOR THE SYNTHESIS OF ORGANOBORON COMPOUNDS .

Degree: PhD, 2017, Princeton University

 The versatility of organoboron compounds in organic synthesis inspires the discovery of efficient and sustainable methods for their synthesis; hence, providing more inexpensive, less toxic,… (more)

Subjects/Keywords: C-H Borylation; Cobalt catalysis; Hydroboration

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APA (6th Edition):

Obligacion, J. V. (2017). BASE METAL CATALYSIS FOR THE SYNTHESIS OF ORGANOBORON COMPOUNDS . (Doctoral Dissertation). Princeton University. Retrieved from http://arks.princeton.edu/ark:/88435/dsp014m90dz102

Chicago Manual of Style (16th Edition):

Obligacion, Jennifer Victoriano. “BASE METAL CATALYSIS FOR THE SYNTHESIS OF ORGANOBORON COMPOUNDS .” 2017. Doctoral Dissertation, Princeton University. Accessed October 21, 2019. http://arks.princeton.edu/ark:/88435/dsp014m90dz102.

MLA Handbook (7th Edition):

Obligacion, Jennifer Victoriano. “BASE METAL CATALYSIS FOR THE SYNTHESIS OF ORGANOBORON COMPOUNDS .” 2017. Web. 21 Oct 2019.

Vancouver:

Obligacion JV. BASE METAL CATALYSIS FOR THE SYNTHESIS OF ORGANOBORON COMPOUNDS . [Internet] [Doctoral dissertation]. Princeton University; 2017. [cited 2019 Oct 21]. Available from: http://arks.princeton.edu/ark:/88435/dsp014m90dz102.

Council of Science Editors:

Obligacion JV. BASE METAL CATALYSIS FOR THE SYNTHESIS OF ORGANOBORON COMPOUNDS . [Doctoral Dissertation]. Princeton University; 2017. Available from: http://arks.princeton.edu/ark:/88435/dsp014m90dz102


Virginia Tech

13. Nelson, Amanda Kay. Metal-Catalyzed Formation and Transformations of Carbon-Boron Bonds.

Degree: PhD, Chemistry, 2016, Virginia Tech

 Our research seeks new methods for functionalizing organic small molecules using organoboronic derivatives as a versatile handle for late-stage manipulations. Metal-catalyzed formation of new carbon-boron… (more)

Subjects/Keywords: borylation; diboration; conjugate addition; aqueous; copper; cross-coupling

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APA (6th Edition):

Nelson, A. K. (2016). Metal-Catalyzed Formation and Transformations of Carbon-Boron Bonds. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/83400

Chicago Manual of Style (16th Edition):

Nelson, Amanda Kay. “Metal-Catalyzed Formation and Transformations of Carbon-Boron Bonds.” 2016. Doctoral Dissertation, Virginia Tech. Accessed October 21, 2019. http://hdl.handle.net/10919/83400.

MLA Handbook (7th Edition):

Nelson, Amanda Kay. “Metal-Catalyzed Formation and Transformations of Carbon-Boron Bonds.” 2016. Web. 21 Oct 2019.

Vancouver:

Nelson AK. Metal-Catalyzed Formation and Transformations of Carbon-Boron Bonds. [Internet] [Doctoral dissertation]. Virginia Tech; 2016. [cited 2019 Oct 21]. Available from: http://hdl.handle.net/10919/83400.

Council of Science Editors:

Nelson AK. Metal-Catalyzed Formation and Transformations of Carbon-Boron Bonds. [Doctoral Dissertation]. Virginia Tech; 2016. Available from: http://hdl.handle.net/10919/83400


University of Manchester

14. Ayuso Carrillo, Josue Israel. Low cost, more efficient, and less toxic synthetic routes to conjugated polymers.

Degree: 2016, University of Manchester

 As key components of flexible organic electronics, the synthesis ofpolythiophenes via less toxic and more cost-effective routes is demanded. Anefficient synthetic route for the production… (more)

Subjects/Keywords: conjugated polymers; Suzuki-Miyaura cross-coupling; Electrophilic borylation; MIDA boronates; slow release; thiophenes; organic electronics

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APA (6th Edition):

Ayuso Carrillo, J. I. (2016). Low cost, more efficient, and less toxic synthetic routes to conjugated polymers. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:302874

Chicago Manual of Style (16th Edition):

Ayuso Carrillo, Josue Israel. “Low cost, more efficient, and less toxic synthetic routes to conjugated polymers.” 2016. Doctoral Dissertation, University of Manchester. Accessed October 21, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:302874.

MLA Handbook (7th Edition):

Ayuso Carrillo, Josue Israel. “Low cost, more efficient, and less toxic synthetic routes to conjugated polymers.” 2016. Web. 21 Oct 2019.

Vancouver:

Ayuso Carrillo JI. Low cost, more efficient, and less toxic synthetic routes to conjugated polymers. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2019 Oct 21]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:302874.

Council of Science Editors:

Ayuso Carrillo JI. Low cost, more efficient, and less toxic synthetic routes to conjugated polymers. [Doctoral Dissertation]. University of Manchester; 2016. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:302874


Texas A&M University

15. Press, Loren Paul. High-Turnover C-H Borylation of Arenes with (POCOP) Iridium Complexes, The Synthesis of Group 9/10 (POCS) Complexes and the Study of Triflyloxy-Substituted Carboranes.

Degree: PhD, Chemistry, 2016, Texas A&M University

 Over the last century, transition metal-catalyzed C-H functionalization has emerged as one of the most important topics in synthetic chemistry. One type of C-H functionalization,… (more)

Subjects/Keywords: C-H functionalization; C-H activation; borylation; POCOP; iridium; POCS; triflyloxy; carboranes; weakly coordinating anions

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APA (6th Edition):

Press, L. P. (2016). High-Turnover C-H Borylation of Arenes with (POCOP) Iridium Complexes, The Synthesis of Group 9/10 (POCS) Complexes and the Study of Triflyloxy-Substituted Carboranes. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/158080

Chicago Manual of Style (16th Edition):

Press, Loren Paul. “High-Turnover C-H Borylation of Arenes with (POCOP) Iridium Complexes, The Synthesis of Group 9/10 (POCS) Complexes and the Study of Triflyloxy-Substituted Carboranes.” 2016. Doctoral Dissertation, Texas A&M University. Accessed October 21, 2019. http://hdl.handle.net/1969.1/158080.

MLA Handbook (7th Edition):

Press, Loren Paul. “High-Turnover C-H Borylation of Arenes with (POCOP) Iridium Complexes, The Synthesis of Group 9/10 (POCS) Complexes and the Study of Triflyloxy-Substituted Carboranes.” 2016. Web. 21 Oct 2019.

Vancouver:

Press LP. High-Turnover C-H Borylation of Arenes with (POCOP) Iridium Complexes, The Synthesis of Group 9/10 (POCS) Complexes and the Study of Triflyloxy-Substituted Carboranes. [Internet] [Doctoral dissertation]. Texas A&M University; 2016. [cited 2019 Oct 21]. Available from: http://hdl.handle.net/1969.1/158080.

Council of Science Editors:

Press LP. High-Turnover C-H Borylation of Arenes with (POCOP) Iridium Complexes, The Synthesis of Group 9/10 (POCS) Complexes and the Study of Triflyloxy-Substituted Carboranes. [Doctoral Dissertation]. Texas A&M University; 2016. Available from: http://hdl.handle.net/1969.1/158080


University of Manchester

16. Crossley, Daniel. Directed C-H Borylation for the Synthesis of Fused and Ladder Type Conjugated Oligomers and Polymers.

Degree: 2016, University of Manchester

The synthesis, photophysical and electronic properties of a series of novel boron containing fused and ladder type donor−acceptor (D-A) oligomers and polymers are reported. The… (more)

Subjects/Keywords: Boron; Donor-Acceptor Compounds; OLEDs; Polymers; Near Infra-red Emission; Organoboron; Direct C-H Electrophilic Borylation

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APA (6th Edition):

Crossley, D. (2016). Directed C-H Borylation for the Synthesis of Fused and Ladder Type Conjugated Oligomers and Polymers. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:301616

Chicago Manual of Style (16th Edition):

Crossley, Daniel. “Directed C-H Borylation for the Synthesis of Fused and Ladder Type Conjugated Oligomers and Polymers.” 2016. Doctoral Dissertation, University of Manchester. Accessed October 21, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:301616.

MLA Handbook (7th Edition):

Crossley, Daniel. “Directed C-H Borylation for the Synthesis of Fused and Ladder Type Conjugated Oligomers and Polymers.” 2016. Web. 21 Oct 2019.

Vancouver:

Crossley D. Directed C-H Borylation for the Synthesis of Fused and Ladder Type Conjugated Oligomers and Polymers. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2019 Oct 21]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:301616.

Council of Science Editors:

Crossley D. Directed C-H Borylation for the Synthesis of Fused and Ladder Type Conjugated Oligomers and Polymers. [Doctoral Dissertation]. University of Manchester; 2016. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:301616


University of Manchester

17. Heard, Kane. Novel Polyaromatics for Organic Electronics and Graphene Exfoliation: Synthetic Approaches Utilising Regioselective Aromatic C-H Borylation.

Degree: 2016, University of Manchester

 Projects were undertaken investigating the functionalisation of polyaromatic cores (chrysene, pyrene and perylene) for use in organic electronics and aqueous graphene stabilisation. In each case… (more)

Subjects/Keywords: Polyaromatic Synthesis; C-H Borylation; Organic Electronics; Graphene Exfoliation

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APA (6th Edition):

Heard, K. (2016). Novel Polyaromatics for Organic Electronics and Graphene Exfoliation: Synthetic Approaches Utilising Regioselective Aromatic C-H Borylation. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:301438

Chicago Manual of Style (16th Edition):

Heard, Kane. “Novel Polyaromatics for Organic Electronics and Graphene Exfoliation: Synthetic Approaches Utilising Regioselective Aromatic C-H Borylation.” 2016. Doctoral Dissertation, University of Manchester. Accessed October 21, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:301438.

MLA Handbook (7th Edition):

Heard, Kane. “Novel Polyaromatics for Organic Electronics and Graphene Exfoliation: Synthetic Approaches Utilising Regioselective Aromatic C-H Borylation.” 2016. Web. 21 Oct 2019.

Vancouver:

Heard K. Novel Polyaromatics for Organic Electronics and Graphene Exfoliation: Synthetic Approaches Utilising Regioselective Aromatic C-H Borylation. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2019 Oct 21]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:301438.

Council of Science Editors:

Heard K. Novel Polyaromatics for Organic Electronics and Graphene Exfoliation: Synthetic Approaches Utilising Regioselective Aromatic C-H Borylation. [Doctoral Dissertation]. University of Manchester; 2016. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:301438


University of Alberta

18. Kim, You-Ri. Optimization and Applications of the Catalytic Enantioselective Borylative Migration of Functionalized Piperidines.

Degree: MS, Department of Chemistry, 2016, University of Alberta

 The catalytic enantioselective borylative migration developed in 2009 by our laboratory is a convenient, single-step method that provides enantiomerically enriched heterocyclic allylboronates. However, this chemistry… (more)

Subjects/Keywords: Piperidine; Borylation; Allylboronate; Allylboration; Chiral piperidine

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APA (6th Edition):

Kim, Y. (2016). Optimization and Applications of the Catalytic Enantioselective Borylative Migration of Functionalized Piperidines. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/c4m90dv69q

Chicago Manual of Style (16th Edition):

Kim, You-Ri. “Optimization and Applications of the Catalytic Enantioselective Borylative Migration of Functionalized Piperidines.” 2016. Masters Thesis, University of Alberta. Accessed October 21, 2019. https://era.library.ualberta.ca/files/c4m90dv69q.

MLA Handbook (7th Edition):

Kim, You-Ri. “Optimization and Applications of the Catalytic Enantioselective Borylative Migration of Functionalized Piperidines.” 2016. Web. 21 Oct 2019.

Vancouver:

Kim Y. Optimization and Applications of the Catalytic Enantioselective Borylative Migration of Functionalized Piperidines. [Internet] [Masters thesis]. University of Alberta; 2016. [cited 2019 Oct 21]. Available from: https://era.library.ualberta.ca/files/c4m90dv69q.

Council of Science Editors:

Kim Y. Optimization and Applications of the Catalytic Enantioselective Borylative Migration of Functionalized Piperidines. [Masters Thesis]. University of Alberta; 2016. Available from: https://era.library.ualberta.ca/files/c4m90dv69q


Kyoto University / 京都大学

19. Kitano, Masaaki. Chemistry of meso-Free Subporphyrins : メゾフリーサブポルフィリンの化学.

Degree: 博士(理学), 2016, Kyoto University / 京都大学

新制・課程博士

甲第19516号

理博第4176号

Subjects/Keywords: porphyrinoids; subporphyrins; cross-coupling reactions; substitution; borylation

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APA (6th Edition):

Kitano, M. (2016). Chemistry of meso-Free Subporphyrins : メゾフリーサブポルフィリンの化学. (Thesis). Kyoto University / 京都大学. Retrieved from http://hdl.handle.net/2433/215329 ; http://dx.doi.org/10.14989/doctor.k19516

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Kitano, Masaaki. “Chemistry of meso-Free Subporphyrins : メゾフリーサブポルフィリンの化学.” 2016. Thesis, Kyoto University / 京都大学. Accessed October 21, 2019. http://hdl.handle.net/2433/215329 ; http://dx.doi.org/10.14989/doctor.k19516.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Kitano, Masaaki. “Chemistry of meso-Free Subporphyrins : メゾフリーサブポルフィリンの化学.” 2016. Web. 21 Oct 2019.

Vancouver:

Kitano M. Chemistry of meso-Free Subporphyrins : メゾフリーサブポルフィリンの化学. [Internet] [Thesis]. Kyoto University / 京都大学; 2016. [cited 2019 Oct 21]. Available from: http://hdl.handle.net/2433/215329 ; http://dx.doi.org/10.14989/doctor.k19516.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Kitano M. Chemistry of meso-Free Subporphyrins : メゾフリーサブポルフィリンの化学. [Thesis]. Kyoto University / 京都大学; 2016. Available from: http://hdl.handle.net/2433/215329 ; http://dx.doi.org/10.14989/doctor.k19516

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Kyoto University

20. Kitano, Masaaki. Chemistry of meso-Free Subporphyrins .

Degree: 2016, Kyoto University

Subjects/Keywords: porphyrinoids; subporphyrins; cross-coupling reactions; substitution; borylation

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APA (6th Edition):

Kitano, M. (2016). Chemistry of meso-Free Subporphyrins . (Thesis). Kyoto University. Retrieved from http://hdl.handle.net/2433/215329

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Kitano, Masaaki. “Chemistry of meso-Free Subporphyrins .” 2016. Thesis, Kyoto University. Accessed October 21, 2019. http://hdl.handle.net/2433/215329.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Kitano, Masaaki. “Chemistry of meso-Free Subporphyrins .” 2016. Web. 21 Oct 2019.

Vancouver:

Kitano M. Chemistry of meso-Free Subporphyrins . [Internet] [Thesis]. Kyoto University; 2016. [cited 2019 Oct 21]. Available from: http://hdl.handle.net/2433/215329.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Kitano M. Chemistry of meso-Free Subporphyrins . [Thesis]. Kyoto University; 2016. Available from: http://hdl.handle.net/2433/215329

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Boston College

21. Xiao, Lu. Copper-Catalyzed Borylation of Hemiaminal Ethers and Ruthenium-Catalyzed Tandem Reactions of Nitrogen-Tethered Dienes.

Degree: PhD, Chemistry, 2016, Boston College

 Chapter 1 Bisphosphine monoxides have unique coordinating capabilities with transition metals. Several research groups have independently reported transition metal-catalyzed highly stereoselective reactions by using chiral… (more)

Subjects/Keywords: Borylation; Catalysis; Copper; Ruthenium; Tandem Reactions

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APA (6th Edition):

Xiao, L. (2016). Copper-Catalyzed Borylation of Hemiaminal Ethers and Ruthenium-Catalyzed Tandem Reactions of Nitrogen-Tethered Dienes. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:107234

Chicago Manual of Style (16th Edition):

Xiao, Lu. “Copper-Catalyzed Borylation of Hemiaminal Ethers and Ruthenium-Catalyzed Tandem Reactions of Nitrogen-Tethered Dienes.” 2016. Doctoral Dissertation, Boston College. Accessed October 21, 2019. http://dlib.bc.edu/islandora/object/bc-ir:107234.

MLA Handbook (7th Edition):

Xiao, Lu. “Copper-Catalyzed Borylation of Hemiaminal Ethers and Ruthenium-Catalyzed Tandem Reactions of Nitrogen-Tethered Dienes.” 2016. Web. 21 Oct 2019.

Vancouver:

Xiao L. Copper-Catalyzed Borylation of Hemiaminal Ethers and Ruthenium-Catalyzed Tandem Reactions of Nitrogen-Tethered Dienes. [Internet] [Doctoral dissertation]. Boston College; 2016. [cited 2019 Oct 21]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:107234.

Council of Science Editors:

Xiao L. Copper-Catalyzed Borylation of Hemiaminal Ethers and Ruthenium-Catalyzed Tandem Reactions of Nitrogen-Tethered Dienes. [Doctoral Dissertation]. Boston College; 2016. Available from: http://dlib.bc.edu/islandora/object/bc-ir:107234


University of Manchester

22. Crossley, Daniel. Directed C-H borylation for the synthesis of fused and ladder type conjugated oligomers and polymers.

Degree: PhD, 2016, University of Manchester

 The synthesis, photophysical and electronic properties of a series of novel boron containing fused and ladder type donor-acceptor (D-A) oligomers and polymers are reported. The… (more)

Subjects/Keywords: 540; Organoboron; Direct C-H Electrophilic Borylation; Near Infra-red Emission; Boron; OLEDs; Donor-Acceptor Compounds; Polymers

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APA (6th Edition):

Crossley, D. (2016). Directed C-H borylation for the synthesis of fused and ladder type conjugated oligomers and polymers. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/directed-ch-borylation-for-the-synthesis-of-fused-and-ladder-type-conjugated-oligomers-and-polymers(8c96a89b-7442-41f3-839b-56148b5fd458).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.748012

Chicago Manual of Style (16th Edition):

Crossley, Daniel. “Directed C-H borylation for the synthesis of fused and ladder type conjugated oligomers and polymers.” 2016. Doctoral Dissertation, University of Manchester. Accessed October 21, 2019. https://www.research.manchester.ac.uk/portal/en/theses/directed-ch-borylation-for-the-synthesis-of-fused-and-ladder-type-conjugated-oligomers-and-polymers(8c96a89b-7442-41f3-839b-56148b5fd458).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.748012.

MLA Handbook (7th Edition):

Crossley, Daniel. “Directed C-H borylation for the synthesis of fused and ladder type conjugated oligomers and polymers.” 2016. Web. 21 Oct 2019.

Vancouver:

Crossley D. Directed C-H borylation for the synthesis of fused and ladder type conjugated oligomers and polymers. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2019 Oct 21]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/directed-ch-borylation-for-the-synthesis-of-fused-and-ladder-type-conjugated-oligomers-and-polymers(8c96a89b-7442-41f3-839b-56148b5fd458).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.748012.

Council of Science Editors:

Crossley D. Directed C-H borylation for the synthesis of fused and ladder type conjugated oligomers and polymers. [Doctoral Dissertation]. University of Manchester; 2016. Available from: https://www.research.manchester.ac.uk/portal/en/theses/directed-ch-borylation-for-the-synthesis-of-fused-and-ladder-type-conjugated-oligomers-and-polymers(8c96a89b-7442-41f3-839b-56148b5fd458).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.748012


University of California – Irvine

23. Issaian, Adena. Carboxyboration: The Catalyst-Free Synthesis of Borylated Lactones and Isocoumarins From Esters.

Degree: Chemistry, 2016, University of California – Irvine

 Catalyst-free formation of isocoumarins and α-pyrones from the corresponding alkynyl esters is realized. The resulting γ- and δ-lactones are isolated as the pinacolboronic esters, boronic… (more)

Subjects/Keywords: Chemistry; borylation; catalyst-free; chlorocatecholborane; cyclization; electrophilic; oxyboration

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APA (6th Edition):

Issaian, A. (2016). Carboxyboration: The Catalyst-Free Synthesis of Borylated Lactones and Isocoumarins From Esters. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/0j63x4r0

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Issaian, Adena. “Carboxyboration: The Catalyst-Free Synthesis of Borylated Lactones and Isocoumarins From Esters.” 2016. Thesis, University of California – Irvine. Accessed October 21, 2019. http://www.escholarship.org/uc/item/0j63x4r0.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Issaian, Adena. “Carboxyboration: The Catalyst-Free Synthesis of Borylated Lactones and Isocoumarins From Esters.” 2016. Web. 21 Oct 2019.

Vancouver:

Issaian A. Carboxyboration: The Catalyst-Free Synthesis of Borylated Lactones and Isocoumarins From Esters. [Internet] [Thesis]. University of California – Irvine; 2016. [cited 2019 Oct 21]. Available from: http://www.escholarship.org/uc/item/0j63x4r0.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Issaian A. Carboxyboration: The Catalyst-Free Synthesis of Borylated Lactones and Isocoumarins From Esters. [Thesis]. University of California – Irvine; 2016. Available from: http://www.escholarship.org/uc/item/0j63x4r0

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Manchester

24. Ayuso Carrillo, Josue. Low cost, more efficient, and less toxic synthetic routes to conjugated polymers.

Degree: PhD, 2016, University of Manchester

 As key components of flexible organic electronics, the synthesis of polythiophenes via less toxic and more cost-effective routes is demanded. An efficient synthetic route for… (more)

Subjects/Keywords: 547; organic electronics; thiophenes; slow release; Electrophilic borylation; MIDA boronates; Suzuki-Miyaura cross-coupling; conjugated polymers

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APA (6th Edition):

Ayuso Carrillo, J. (2016). Low cost, more efficient, and less toxic synthetic routes to conjugated polymers. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/low-cost-more-efficient-and-less-toxic-synthetic-routes-to-conjugated-polymers(ee15f7a0-39da-46e8-b512-ff3fb33e4f06).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.727930

Chicago Manual of Style (16th Edition):

Ayuso Carrillo, Josue. “Low cost, more efficient, and less toxic synthetic routes to conjugated polymers.” 2016. Doctoral Dissertation, University of Manchester. Accessed October 21, 2019. https://www.research.manchester.ac.uk/portal/en/theses/low-cost-more-efficient-and-less-toxic-synthetic-routes-to-conjugated-polymers(ee15f7a0-39da-46e8-b512-ff3fb33e4f06).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.727930.

MLA Handbook (7th Edition):

Ayuso Carrillo, Josue. “Low cost, more efficient, and less toxic synthetic routes to conjugated polymers.” 2016. Web. 21 Oct 2019.

Vancouver:

Ayuso Carrillo J. Low cost, more efficient, and less toxic synthetic routes to conjugated polymers. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2019 Oct 21]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/low-cost-more-efficient-and-less-toxic-synthetic-routes-to-conjugated-polymers(ee15f7a0-39da-46e8-b512-ff3fb33e4f06).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.727930.

Council of Science Editors:

Ayuso Carrillo J. Low cost, more efficient, and less toxic synthetic routes to conjugated polymers. [Doctoral Dissertation]. University of Manchester; 2016. Available from: https://www.research.manchester.ac.uk/portal/en/theses/low-cost-more-efficient-and-less-toxic-synthetic-routes-to-conjugated-polymers(ee15f7a0-39da-46e8-b512-ff3fb33e4f06).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.727930


University of Manchester

25. Heard, Kane. Novel polyaromatics for organic electronics and graphene exfoliation : synthetic approaches utilising regioselective aromatic C-H borylation.

Degree: PhD, 2016, University of Manchester

 Projects were undertaken investigating the functionalisation of polyaromatic cores (chrysene, pyrene and perylene) for use in organic electronics and aqueous graphene stabilisation. In each case… (more)

Subjects/Keywords: 547; Polyaromatic Synthesis; C-H Borylation; Organic Electronics; Graphene Exfoliation

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Heard, K. (2016). Novel polyaromatics for organic electronics and graphene exfoliation : synthetic approaches utilising regioselective aromatic C-H borylation. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/novel-polyaromatics-for-organic-electronics-and-graphene-exfoliation-synthetic-approaches-utilising-regioselective-aromatic-ch-borylation(f8cd1879-521e-41f6-8a3c-2af7add7844b).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.727929

Chicago Manual of Style (16th Edition):

Heard, Kane. “Novel polyaromatics for organic electronics and graphene exfoliation : synthetic approaches utilising regioselective aromatic C-H borylation.” 2016. Doctoral Dissertation, University of Manchester. Accessed October 21, 2019. https://www.research.manchester.ac.uk/portal/en/theses/novel-polyaromatics-for-organic-electronics-and-graphene-exfoliation-synthetic-approaches-utilising-regioselective-aromatic-ch-borylation(f8cd1879-521e-41f6-8a3c-2af7add7844b).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.727929.

MLA Handbook (7th Edition):

Heard, Kane. “Novel polyaromatics for organic electronics and graphene exfoliation : synthetic approaches utilising regioselective aromatic C-H borylation.” 2016. Web. 21 Oct 2019.

Vancouver:

Heard K. Novel polyaromatics for organic electronics and graphene exfoliation : synthetic approaches utilising regioselective aromatic C-H borylation. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2019 Oct 21]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/novel-polyaromatics-for-organic-electronics-and-graphene-exfoliation-synthetic-approaches-utilising-regioselective-aromatic-ch-borylation(f8cd1879-521e-41f6-8a3c-2af7add7844b).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.727929.

Council of Science Editors:

Heard K. Novel polyaromatics for organic electronics and graphene exfoliation : synthetic approaches utilising regioselective aromatic C-H borylation. [Doctoral Dissertation]. University of Manchester; 2016. Available from: https://www.research.manchester.ac.uk/portal/en/theses/novel-polyaromatics-for-organic-electronics-and-graphene-exfoliation-synthetic-approaches-utilising-regioselective-aromatic-ch-borylation(f8cd1879-521e-41f6-8a3c-2af7add7844b).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.727929


Queens University

26. Cosman, Jennifer. Advances in Metal-Catalyzed C–H Borylation and Multicomponent Allylic Substitution Reactions .

Degree: Chemistry, 2015, Queens University

 Chapter one of this thesis describes the iridium-catalyzed ortho-selective C–H borylation reaction of tertiary benzamides. An iridium(I) complex paired with an electron-deficient phosphine ligand allows… (more)

Subjects/Keywords: multicomponent reactions; C-H activation; allylic substitution; Mizoroki-Heck reaction; iridium-catalyzed C-H borylation

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Cosman, J. (2015). Advances in Metal-Catalyzed C–H Borylation and Multicomponent Allylic Substitution Reactions . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/13534

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Cosman, Jennifer. “Advances in Metal-Catalyzed C–H Borylation and Multicomponent Allylic Substitution Reactions .” 2015. Thesis, Queens University. Accessed October 21, 2019. http://hdl.handle.net/1974/13534.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Cosman, Jennifer. “Advances in Metal-Catalyzed C–H Borylation and Multicomponent Allylic Substitution Reactions .” 2015. Web. 21 Oct 2019.

Vancouver:

Cosman J. Advances in Metal-Catalyzed C–H Borylation and Multicomponent Allylic Substitution Reactions . [Internet] [Thesis]. Queens University; 2015. [cited 2019 Oct 21]. Available from: http://hdl.handle.net/1974/13534.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Cosman J. Advances in Metal-Catalyzed C–H Borylation and Multicomponent Allylic Substitution Reactions . [Thesis]. Queens University; 2015. Available from: http://hdl.handle.net/1974/13534

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Universitat Rovira i Virgili

27. Palau Lluch, Gerard. alpha,beta-difunctionalization of alpha,beta-unsaturated carbonyl compounds through borylation reaction.

Degree: Departament de Química Física i Inorgànica, 2015, Universitat Rovira i Virgili

 This thesis presents the results concerning new methodologies towards the obtantion of alpha-functionalized beta-borylated compounds from alpha,beta-unsaturated carbonyl compounds, with no precedent in the litherature.… (more)

Subjects/Keywords: Borilació; Halogenació; Difuncionalització; Borilación; Halogenación; Difuncionalización; Borylation; Halogenation; Difunctionalization; 54; 546; 547; 6

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Palau Lluch, G. (2015). alpha,beta-difunctionalization of alpha,beta-unsaturated carbonyl compounds through borylation reaction. (Thesis). Universitat Rovira i Virgili. Retrieved from http://hdl.handle.net/10803/311620

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Palau Lluch, Gerard. “alpha,beta-difunctionalization of alpha,beta-unsaturated carbonyl compounds through borylation reaction.” 2015. Thesis, Universitat Rovira i Virgili. Accessed October 21, 2019. http://hdl.handle.net/10803/311620.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Palau Lluch, Gerard. “alpha,beta-difunctionalization of alpha,beta-unsaturated carbonyl compounds through borylation reaction.” 2015. Web. 21 Oct 2019.

Vancouver:

Palau Lluch G. alpha,beta-difunctionalization of alpha,beta-unsaturated carbonyl compounds through borylation reaction. [Internet] [Thesis]. Universitat Rovira i Virgili; 2015. [cited 2019 Oct 21]. Available from: http://hdl.handle.net/10803/311620.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Palau Lluch G. alpha,beta-difunctionalization of alpha,beta-unsaturated carbonyl compounds through borylation reaction. [Thesis]. Universitat Rovira i Virgili; 2015. Available from: http://hdl.handle.net/10803/311620

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

28. Moore, Brandon. HIGHLY SELECTIVE RHODIUM-CATALYZED C-H BORYLATIONS IN PREPARATION OF SUBSTRATES FOR SUZUKI-MIYAURA CROSS-COUPLINGS: MONO- AND CHEMOSELECTIVE FORMATION OF AROMATIC COMPOUNDS .

Degree: Chemistry, 2015, Queens University

 The advent of the Suzuki–Miyaura cross–coupling reaction and its significance to the synthesis of new carbon–carbon bonds has increased the demand for efficient routes to… (more)

Subjects/Keywords: Cross-Coupling; Suzuki; Borylation; Heck; Transition Metal; C-H Activation; Palladium; Boronic Ester; Catalysis; Carbenes; Chemoselective; Regioselective; NHC; Arylation; Boron; Rhodium

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Moore, B. (2015). HIGHLY SELECTIVE RHODIUM-CATALYZED C-H BORYLATIONS IN PREPARATION OF SUBSTRATES FOR SUZUKI-MIYAURA CROSS-COUPLINGS: MONO- AND CHEMOSELECTIVE FORMATION OF AROMATIC COMPOUNDS . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/12795

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Moore, Brandon. “HIGHLY SELECTIVE RHODIUM-CATALYZED C-H BORYLATIONS IN PREPARATION OF SUBSTRATES FOR SUZUKI-MIYAURA CROSS-COUPLINGS: MONO- AND CHEMOSELECTIVE FORMATION OF AROMATIC COMPOUNDS .” 2015. Thesis, Queens University. Accessed October 21, 2019. http://hdl.handle.net/1974/12795.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Moore, Brandon. “HIGHLY SELECTIVE RHODIUM-CATALYZED C-H BORYLATIONS IN PREPARATION OF SUBSTRATES FOR SUZUKI-MIYAURA CROSS-COUPLINGS: MONO- AND CHEMOSELECTIVE FORMATION OF AROMATIC COMPOUNDS .” 2015. Web. 21 Oct 2019.

Vancouver:

Moore B. HIGHLY SELECTIVE RHODIUM-CATALYZED C-H BORYLATIONS IN PREPARATION OF SUBSTRATES FOR SUZUKI-MIYAURA CROSS-COUPLINGS: MONO- AND CHEMOSELECTIVE FORMATION OF AROMATIC COMPOUNDS . [Internet] [Thesis]. Queens University; 2015. [cited 2019 Oct 21]. Available from: http://hdl.handle.net/1974/12795.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Moore B. HIGHLY SELECTIVE RHODIUM-CATALYZED C-H BORYLATIONS IN PREPARATION OF SUBSTRATES FOR SUZUKI-MIYAURA CROSS-COUPLINGS: MONO- AND CHEMOSELECTIVE FORMATION OF AROMATIC COMPOUNDS . [Thesis]. Queens University; 2015. Available from: http://hdl.handle.net/1974/12795

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Texas A&M University

29. Lee, Chun-I. C-H Borylation Mediated by Group 9 Pincer Complexes and Synthesis of Iridium Triflates and Triarylmethyl Species.

Degree: 2015, Texas A&M University

 The importance of organoboron compounds in chemical synthesis is apparent from the Nobel Prizes awarded to Herbert C. Brown (1979) and Akira Suzuki (2010) for… (more)

Subjects/Keywords: pincer complex; iridium; rhodium; borylation; alkyne; alkynylboronate; trityl

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Lee, C. (2015). C-H Borylation Mediated by Group 9 Pincer Complexes and Synthesis of Iridium Triflates and Triarylmethyl Species. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/161242

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Lee, Chun-I. “C-H Borylation Mediated by Group 9 Pincer Complexes and Synthesis of Iridium Triflates and Triarylmethyl Species.” 2015. Thesis, Texas A&M University. Accessed October 21, 2019. http://hdl.handle.net/1969.1/161242.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Lee, Chun-I. “C-H Borylation Mediated by Group 9 Pincer Complexes and Synthesis of Iridium Triflates and Triarylmethyl Species.” 2015. Web. 21 Oct 2019.

Vancouver:

Lee C. C-H Borylation Mediated by Group 9 Pincer Complexes and Synthesis of Iridium Triflates and Triarylmethyl Species. [Internet] [Thesis]. Texas A&M University; 2015. [cited 2019 Oct 21]. Available from: http://hdl.handle.net/1969.1/161242.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Lee C. C-H Borylation Mediated by Group 9 Pincer Complexes and Synthesis of Iridium Triflates and Triarylmethyl Species. [Thesis]. Texas A&M University; 2015. Available from: http://hdl.handle.net/1969.1/161242

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

30. Solana González, Jorge. Copper and iridium conjugate addition : cyclisation processes, domino reactions.

Degree: PhD, 2015, University of Edinburgh

 Asymmetric conjugate addition of bis(pinacolato)diboron followed by aldol cyclisation of enone diones under the action of a chiral copper catalyst has been developed. This enantioselective… (more)

Subjects/Keywords: 546; domino reactions; iridium; copper; borylation

…13 2.2 Copper-Catalysed Asymmetric Conjugate Borylation… …chlorides in the presence of Xantphos (L03), the borylation occurred exclusively on the… …copper-Xantphos catalyst performs the borylation on the unactivated alkene forming alkyl-copper… …compound 25 (Scheme 5). Scheme 5: Copper domino borylation/cyclisation process… …reported. Similarly as Ito (Scheme 6), Lin’s group applied borylation conditions with a… 

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Solana González, J. (2015). Copper and iridium conjugate addition : cyclisation processes, domino reactions. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/10471

Chicago Manual of Style (16th Edition):

Solana González, Jorge. “Copper and iridium conjugate addition : cyclisation processes, domino reactions.” 2015. Doctoral Dissertation, University of Edinburgh. Accessed October 21, 2019. http://hdl.handle.net/1842/10471.

MLA Handbook (7th Edition):

Solana González, Jorge. “Copper and iridium conjugate addition : cyclisation processes, domino reactions.” 2015. Web. 21 Oct 2019.

Vancouver:

Solana González J. Copper and iridium conjugate addition : cyclisation processes, domino reactions. [Internet] [Doctoral dissertation]. University of Edinburgh; 2015. [cited 2019 Oct 21]. Available from: http://hdl.handle.net/1842/10471.

Council of Science Editors:

Solana González J. Copper and iridium conjugate addition : cyclisation processes, domino reactions. [Doctoral Dissertation]. University of Edinburgh; 2015. Available from: http://hdl.handle.net/1842/10471

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